CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 37 enrolled
Drug / intervention
Core Exercise Promotion Interventionbehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04903249
NCT04903249N/ACompleted

Increasing Physical Activity Among Breast Cancer Survivors: Use of the ORBIT Model to Refine and Test a Novel Approach to Exercise Promotion Based on Affect-regulation

Dartmouth-Hitchcock Medical Center·interventional·Posted May 26, 2021·Updated Jul 27, 2023

In Brief

A clinical study evaluating Core Exercise Promotion Intervention for Breast Cancer. Completed, enrolled 37 participants across 1 site.

Detailed Summary

The purpose of this study is to refine the use of an affect-regulated exercise prescription for use with survivors of breast cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsBreast Cancer
CountriesUnited States

Timeline

N/ACompletedFinished
20222023202420252026
First PostedMay 26, 2021
Enrollment StartAug 10, 2021
Primary CompletionJun 10, 2022
Study CompletionJun 13, 2022
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 5.1 years ago

Interventions

Core Exercise Promotion Interventionbehavioral

Participants are instructed to increase weekly time spent exercising to \>90 minutes over 12 weeks. Exercise will be defined as "activities that use large muscle groups, increase heart rate and breathing rate, and are performed intentionally for the purpose of exercise (as opposed to physical activities of daily living, e.g., housework). Participants complete a videoconferencing visit with the study team and are given task and safety related information pertaining to exercise for survivors of cancer. Participants engage in exercise-related goal-setting and action planning and are provided activity trackers to monitor their activity levels over the 12-week study period.